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dc.contributor.authorIrvine, Elizabeth A.-
dc.contributor.authorTaylor, Duncan-
dc.date.accessioned2025-04-24T09:40:08Z-
dc.date.available2025-04-24T09:40:08Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18769-
dc.description.abstractThe dehydrogenation and concurrent isomerization of the three n-butenes have been investigated at 474 K on a range of mixed tin + antimony oxide catalysts outgassed at 698 K. The initial approximately zero order reaction rates were used as a measure of catalytic activity to construct patterns of activity as a function of catalyst composition. Comparison of the patterns with those for the isomerization of 3,3-dimethylbut-1-ene and for the selective oxidation of propene on the same catalysts indicate that dehydrogenation of but-1-ene involves a π-allyl intermediate, while isomerization occurs through carbonium ion formation. For the cis- and trans-isomers, it is suggested that both reactions occur via a common allyl (but not π-allyl) type of intermediate.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (06)en_US
dc.subjectChemistryen_US
dc.subjectDehydrogenation of n-butenesen_US
dc.subjectIsomerization of n-butenesen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleDehydrogenation and isomerization of n-butenes on mixed tin + antimony oxide catalystsen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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